Comments on ‘Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’.
Abstract: No abstract available
Publication Date: 2021-10-07 PubMed ID: 34611935DOI: 10.1111/evj.13504Google Scholar: Lookup
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- Comment
Cite This Article
APA
McMullen RJ.
(2021).
Comments on ‘Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse’.
Equine Vet J, 53(6), 1296.
https://doi.org/10.1111/evj.13504 Publication
Researcher Affiliations
- Department of Clinical Sciences, Auburn University, College of Veterinary Medicine, Auburn, AL, USA.
MeSH Terms
- Animals
- Eye Diseases, Hereditary / veterinary
- Genetic Diseases, X-Linked
- Horse Diseases / genetics
- Horses
- Mutation, Missense
- Myopia
- Night Blindness / genetics
- Night Blindness / veterinary
- Tennessee
References
This article includes 3 references
- Hack YL, Crabtree EE, Avila F, Sutton RB, Grahn R, Oh A. Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Equine Vet J 2021;53:316-23.
- Corboy JM. A review of optics. In: Corboy JM, editor. The Retinoscopy Book. Thorofare: SLACK Incorporated, 2003; p. 17-23.
- Bracun A, Ellis AD, Hall C. A retinoscopic survey of 333 horses and ponies in the UK. Vet Ophthalmol 2014;17(Suppl 1):90-6.
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